A novel group of highly hydroxylated steroids from the starfish Protoreaster nodosus
- 1 January 1982
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 38 (24) , 3615-3622
- https://doi.org/10.1016/0040-4020(82)80069-0
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- 5α-cholestane-3β,6β,15α,16β,26-pentol: a polyhydroxylated sterol from the starfish Hacelia attenuataTetrahedron Letters, 1982
- Additivity relation found in the amplitudes of exciton-split circular dichroism curves of pyranose benzoatesJournal of the American Chemical Society, 1981
- 13C n.m.r. spectra of steroids —a survey and commentaryMagnetic Resonance in Chemistry, 1977
- Chemical studies of marine invertebrates. XXIX (1)(1)For part XXVIII see J.C. BRAEKHAN, D. DALOZE, R. SCHUBERT, M. ALBERICCI, B. Tursch, Tetrahedron, in press.Steroids, 1977
- Additivity relations in carbon-13 nuclear magnetic resonance spectra of dihydroxy steroidsThe Journal of Organic Chemistry, 1977
- Oxidation of sterically hindered alcohols to carbonyls with dimethyl sulfoxide-trifluoracetic anhydrideThe Journal of Organic Chemistry, 1976
- Carbon-13 nuclear magnetic resonance spectra of hydroxy steroidsThe Journal of Organic Chemistry, 1976
- Quantitative definition of exciton chirality and the distant effect in the exciton chirality methodJournal of the American Chemical Society, 1975
- Protonenresonanzspektrosopie und Steroidstruktur. II. Die Lage der C‐18‐ und C‐19‐Methylsignale in Abhängigkeit von den Substituenten am SteroidgerüstHelvetica Chimica Acta, 1962